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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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A 6-Year-Old Girl with Progressive Toe Walking
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A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
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Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
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Functional Gait Disorders
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IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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A Demure Teenager and Her Dystonic Foot
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Huntington Disease: Clinical Features and Diagnosis
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Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
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Autopsy Case of Severe Generalized Dystonia and Static Ataxia with Marked Cerebellar Atrophy
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Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
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Criteria for the Diagnosis of Corticobasal Degeneration
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Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
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Rapidly Progressive Corticobasal Degeneration Syndrome
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
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High Doses of Deferiprone May Be Associated with Cerebellar Syndrome
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Progressive Supranuclear Palsy: A Current Review
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Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
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Dopamine-Responsive Dystonia
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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Niemann-Pick Disease Type C: Two Cases and an Update
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Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms
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Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
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Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
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Mitochondrial DNA and Disease
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Long-Term Botulinum Toxin Treatment of Focal Hand Dystonia
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Movement Disorders with Cerebral Toxoplasmosis and AIDS
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Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
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Clinicopath Conf
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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Wilson Disease
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Wilson's Disease:The Problem of Delayed Diagnosis
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Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Extrapyramidal Involvement in Rett's Syndrome
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